ライフサイエンスコーパス: post inoculation

1 cultivar IP18292 with a ~tenfold peak at 9 h post inoculation.

2 318 functional direct target genes at 14 hr post inoculation.

3 s significantly increased between 8-12 weeks post inoculation.

4 f the wheat bran particles after 20 and 40 h post inoculation.

5 uantified infection load on day 8 and day 15 post-inoculation.

6 either kept constant or decreased after 72h post-inoculation.

7 mixed with S. intermedius (P < 10-6) 7 days post-inoculation.

8 ioamnionitis and fetal pathology at 72 hours post-inoculation.

9 he severity of disease from 42 until 84 days post-inoculation.

10 wer in the Sp-a(-/-) mice at all time points post-inoculation.

11 rongly and similarly induced 3 hrs and 1 day post-inoculation.

12 tected in TCV-hp-inoculated leaves at 2 days post-inoculation.

13 d to expand in both ecotypes through 10 days post-inoculation.

14 Importantly, ototopical post-inoculation administration of a PDE4 inhibitor supp

15 ations were maintained for at least 4 months post inoculation, although the levels decreased as the c

16 nd IBD in mdr1a-/- mice within 6 to 17 weeks post-inoculation and before the expected onset of sponta

17 II insert was stable for at least 18-30 days post-inoculation and had little effect on WSMV CP accumu

18 ensitized during the acute infection (3-days post inoculation) and then chronically underwent challen

19 s (BIGs), 462 were induced at or before 36 h post-inoculation, and may be involved in resistance to t

20 ter studies indicated that as early as 1 day post-inoculation, both transcription factor genes were u

21 crosis and limited chlorosis within 5-6 days post-inoculation (d.p.i.), which can lead to systemic ne

22 ignificantly shorter duration of shedding in post-inoculation day 10 subgroup and lower cumulative sh

23 e collected at 30, 60, 90, 105, and 120 days post inoculation (dpi) or at the onset of clinical signs

24 uc, and their tissues were assayed 3-21 days post-inoculation (dpi) for luciferase protein production

25 accumulation at 7 but not at 14 and 21 days post-inoculation (dpi) on the non-inoculated leaves of C

26 At 21 days post-inoculation (dpi), a 76% reduction of linamarin con

27 at the termination of the trials 25-29 days post-inoculation (Flec: 2.2 (2.4), Veh: 4.2 (4.2), P < 0

28 s were circular in profile and within 3 days post-inoculation had developed a brightly fluorescent le

29 Falpha and KC/GRO) was observed at two hours post-inoculation; however, cytokines returned to baselin

30 ponding to defined stages between 1 and 72 h post inoculation (hpi).

31 gen-processing pathways were induced at 24 h post-inoculation (hpi) and/or 48 hpi, while apoptosis an

32 ified as being modulated by TTEs within 12 h post-inoculation (hpi), 20% of which represented transcr

33 nsis adhered to passing nematodes within 8 h post-inoculation (hpi), formed an infection peg between

34 ant viruses were rapidly eliminated 1-7 days post-inoculation in competition experiments with WT.

35 Resistance at 7 days post-inoculation in these accessions was characterized b

36 rease in viral population diversity at day 3 post inoculation is associated with a tenfold reduced le

37 ited increased resistance to BPH only at 3 d post-inoculation of Xoo, while the Xoo infection did not

38 mock-infected corneas were compared at 1 day post inoculation (p.i.) with a murine gene microarray.

39 After a 5-day post-inoculation period, infected presumed motoneurons w

40 gy, and cytokine profiles at 6 and 19 months post inoculation (pi).

41 raesuis at acute (8 hours (h), 24 h and 48 h post-inoculation (pi)) and chronic stages (21 days (d) p

42 jection with PRV, the animals survived 4-day post-inoculation prior to sacrifice and tissue processin

43 leaves displaying HR lesions at 90 and 168 h post-inoculation, salicylate accumulation was detected p

44 Dg93 mRNA is abundant in nodules at 4 weeks post inoculation, the earliest time assayed, and steady-

45 1 and Sgt1, is triggered between 16 and 20 h post inoculation, the same time frame that haustoria of

46 the spinal cords of these animals at 8-12 h post inoculation; this returned to background by 72 h.

47 We used the number of days post inoculation to clinical disease to calculate the in

48 ionally, feces were collected for seven days post-inoculation to determine the effect on gut bacteria

49 Within 30 days post-inoculation, tumors in KO mice were larger than tho

50 paroscopic evaluations for four weeks and at post-inoculation week 8, to monitor upper tract infectio

51 istinct murine models of IPA on days 2 and 3 post inoculation when infection is established and activ

52 enylpropanoid genes analysed occurred at 48h post-inoculation, when decay symptoms started to appear,

53 y in nodule development, between 12 and 96 h post inoculation with Bradyrhizobium japonicum.

54 mes higher than that in wild-type plants 6 h post inoculation with the virulent powdery mildew Golovi

55 At 6 days post-inoculation with nod signal, ENOD40 expression was

56 After 6 wk post-inoculation with Rhizophagus irregularis, root deve